Canonical Allele Identifier: CA14756932

Gene: TOP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.41043978T>A , CM000682.2:g.41043978T>A	GRCh38
NC_000020.10:g.39672618T>A , CM000682.1:g.39672618T>A	GRCh37
NC_000020.9:g.39106032T>A	NCBI36
NG_012262.1:g.20157T>A
NG_012262.2:g.20157T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361337.3:c.58+14523T>A MANE Select	ENSP00000354522.2:n.58+14523T>A
ENST00000681058.1:n.212+14523T>A
ENST00000681113.1:c.58+14523T>A	ENSP00000505788.1:n.58+14523T>A
ENST00000361337.2:c.58+14523T>A	ENSP00000354522.2:n.58+14523T>A
NM_003286.2:c.58+14523T>A	NP_003277.1:n.58+14523T>A
NM_003286.3:c.58+14523T>A	NP_003277.1:n.58+14523T>A
NM_003286.4:c.58+14523T>A MANE Select	NP_003277.1:n.58+14523T>A